A subset of methylated CpG sites differentiate psoriatic from normal skin.

Psoriasis is a chronic inflammatory immune-mediated disorder affecting the skin and other organs including joints. Over 1,300 transcripts are altered in psoriatic involved skin compared with normal skin. However, to our knowledge, global epigenetic profiling of psoriatic skin is previously unreported. Here, we describe a genome-wide study of altered CpG methylation in psoriatic skin. We determined the methylation levels at 27,578 CpG sites in skin samples from individuals with psoriasis (12 involved, 8 uninvolved) and 10 unaffected individuals. CpG methylation of involved skin differed from normal skin at 1,108 sites. Twelve mapped to the epidermal differentiation complex, upstream or within genes that are highly upregulated in psoriasis. Hierarchical clustering of 50 of the top differentially methylated (DM) sites separated psoriatic from normal skin samples with uninvolved skin exhibiting intermediate methylation. CpG sites where methylation was correlated with gene expression are reported. Sites with inverse correlations between methylation and nearby gene expression include those of KYNU, OAS2, S100A12, and SERPINB3, whose strong transcriptional upregulation is an important discriminator of psoriasis. Pyrosequencing of bisulfite-treated DNA from skin biopsies at three DM loci confirmed earlier findings and revealed reversion of methylation levels toward the non-psoriatic state after 1 month of anti-TNF-α therapy

Efficient Hybrid Transformer: Learning Global-local Context for Urban Scene Segmentation

Semantic segmentation of fine-resolution urban scene images plays a vital role in extensive practical applications, such as land cover mapping, urban change detection, environmental protection and economic assessment. Driven by rapid developments in deep learning technologies, the convolutional neural network (CNN) has dominated the semantic segmentation task for many years. Convolutional neural networks adopt hierarchical feature representation, demonstrating strong local information extraction. However, the local property of the convolution layer limits the network from capturing global context that is crucial for precise segmentation. Recently, Transformer comprise a hot topic in the computer vision domain. Transformer demonstrates the great capability of global information modelling, boosting many vision tasks, such as image classification, object detection and especially semantic segmentation. In this paper, we propose an efficient hybrid Transformer (EHT) for real-time urban scene segmentation. The EHT adopts a hybrid structure with and CNN-based encoder and a transformer-based decoder, learning global-local context with lower computation. Extensive experiments demonstrate that our EHT has faster inference speed with competitive accuracy compared with state-of-the-art lightweight models. Specifically, the proposed EHT achieves a 66.9% mIoU on the UAVid test set and outperforms other benchmark networks significantly. The code will be available soon

Remote Estimation of Rice Yield With Unmanned Aerial Vehicle (UAV) Data and Spectral Mixture Analysis

The accurate assessment of rice yield is crucially important for China’s food security and sustainable development. Remote sensing (RS), as an emerging technology, is expected to be useful for rice yield estimation especially at regional scales. With the development of unmanned aerial vehicles (UAVs), a novel approach for RS has been provided, and it is possible to acquire high spatio-temporal resolution imagery on a regional scale. Previous reports have shown that the predictive ability of vegetation index (VI) decreased under the influence of panicle emergence during the later stages of rice growth. In this study, a new approach which integrated UAV-based VI and abundance information obtained from spectral mixture analysis (SMA) was established to improve the estimation accuracy of rice yield at heading stage. The six-band image of all studied rice plots was collected by a camera system mounted on an UAV at booting stage and heading stage respectively. And the corresponding ground measured data was also acquired at the same time. The relationship of several widely-used VIs and Rice Yield was tested at these two stages and a relatively weaker correlation between VI and yield was found at heading stage. In order to improve the estimation accuracy of rice yield at heading stage, the plot-level abundance of panicle, leaf and soil, indicating the fraction of different components within the plot, was derived from SMA on the six-band image and in situ endmember spectra collected for different components. The results showed that VI incorporated with abundance information exhibited a better predictive ability for yield than VI alone. And the product of VI and the difference of leaf abundance and panicle abundance was the most accurate index to reliably estimate yield for rice under different nitrogen treatments at heading stage with the coefficient of determination reaching 0.6 and estimation error below 10%

Oncogenic mutations in GNAQ occur early in uveal melanoma.

PURPOSE: Early/initiating oncogenic mutations have been identified for many cancers, but such mutations remain unidentified in uveal melanoma (UM). An extensive search for such mutations was undertaken, focusing on the RAF/MEK/ERK pathway, which is often the target of initiating mutations in other types of cancer. METHODS: DNA samples from primary UMs were analyzed for mutations in 24 potential oncogenes that affect the RAF/MEK/ERK pathway. For GNAQ, a stimulatory α(q) G-protein subunit which was recently found to be mutated in uveal melanomas, re-sequencing was expanded to include 67 primary UMs and 22 peripheral blood samples. GNAQ status was analyzed for association with clinical, pathologic, chromosomal, immunohistochemical and transcriptional features. RESULTS: Activating mutations at codon 209 were identified in GNAQ in 33/67 (49%) primary UMs, including 2/9 (22%) iris melanomas and 31/58 (54%) posterior UMs. No mutations were found in the other 23 potential oncogenes. GNAQ mutations were not found in normal blood DNA samples. Consistent with GNAQ mutation being an early or initiating event, this mutation was not associated with any clinical, pathologic or molecular features associated with late tumor progression. CONCLUSIONS: GNAQ mutations occur in about half of UMs, representing the most common known oncogenic mutation in this cancer. The presence of this mutation in tumors at all stages of malignant progression suggests that it is an early event in UM. Mutations in this G-protein provide new insights into UM pathogenesis and could lead to new therapeutic possibilities

QTL Mapping of Six Spike and Stem Traits in Hybrid Population of Agropyron Gaertn. in Multiple Environments

Most Agropyron Gaertn. species are excellent sources of forage. The derivative lines of wheat-Agropyron cristatum show elite agronomic traits, and some are valuable for wheat breeding. The species of Agropyron Gaertn. was mainly recognized by the spike morphology in traditional taxon. Six traits, including spike length (SL), ear stem length (ESL), the second internodes length (SIL), spikelet number per spike (SNS), floret number per spikelet (FNS), and grain number per spikelet (GNS), are vital to morphology studies and also influences the forage crop yield. To elucidate the genetic basis of spike and stem traits, a quantitative trait locus (QTL) analysis was conducted in a cross-pollinated (CP) hybrid population derived from a cross between two diverse parents, Agropyron mongolicum Keng Z2098 and A. cristatum (L.) Gaertn. Z1842, evaluated across three ecotopes (Langfang, Changli, and Guyuan of Hebei, China) over 3 years (from 2014 to 2016). Construction of a high-density linkage map was based on 1,023 single-nucleotide polymorphism (SNP) markers, covering 907.8 cM of the whole Agropyron genome. A total of 306 QTLs with single QTL in different environments explaining 0.07–33.21% of the phenotypic variation were detected for study traits. Seven major-effect QTLs were identified, including one for ESL on chromosome 3, one for SIL on chromosome 5, three for SL (two on chromosome 2 and one on chromosome 4), and two for SNS on chromosomes 3 and 7. Also, seven stable QTLs, including four for ESL, one for SL, one for GNS, and one for FNS, were mainly mapped on chromosomes 2, 3, 4, 5, and 7, respectively, elucidating 0.25–14.98% of the phenotypic variations. On the use of Agropyron CP hybrid population to identify QTL determining spike and stem traits for the first time, these QTLs for six traits would provide a theoretical reference for the molecular marker-assisted selection in the improvement of forage and cereal crop species

Juvenile Paget’s Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor Sp7)

Juvenile Paget's disease (JPD) became in 1974 the commonly used name for ultra-rare heritable occurrences of rapid bone remodeling throughout of the skeleton that present in infancy or early childhood as fractures and deformity hallmarked biochemically by marked elevation of serum alkaline phosphatase (ALP) activity (hyperphosphatasemia). Untreated, JPD can kill during childhood or young adult life. In 2002, we reported that homozygous deletion of the gene called tumor necrosis factor receptor superfamily, member 11B (TNFRSF11B) encoding osteoprotegerin (OPG) explained JPD in Navajos. Soon after, other bi-allelic loss-of-function TNFRSF11B defects were identified in JPD worldwide. OPG inhibits osteoclastogenesis and osteoclast activity by decoying receptor activator of nuclear factor κ-B (RANK) ligand (RANKL) away from its receptor RANK. Then, in 2014, we reported JPD in a Bolivian girl caused by a heterozygous activating duplication within TNFRSF11A encoding RANK. Herein, we identify mutation of a third gene underlying JPD. An infant girl began atraumatic fracturing of her lower extremity long-bones. Skull deformity and mild hearing loss followed. Our single investigation of the patient, when she was 15 years-of-age, showed generalized osteosclerosis and hyperostosis. DXA revealed a Z-score of +5.1 at her lumbar spine and T-score of +3.3 at her non-dominant wrist. Biochemical studies were consistent with positive mineral balance and several markers of bone turnover were elevated and included striking hyperphosphatasemia. Iliac crest histopathology was consistent with rapid skeletal remodeling. Measles virus transcripts, common in classic Paget's disease of bone, were not detected in circulating mononuclear cells. Then, reportedly, she responded to several months of alendronate therapy with less skeletal pain and correction of hyperphosphatasemia but had been lost to our follow-up. After we detected no defect in TNFRSF11A or B, trio exome sequencing revealed a de novo heterozygous missense mutation (c.926C>G; p.S309W) within SP7 encoding the osteoblast transcription factor osterix (specificity protein 7, transcription factor SP7). Thus, mutation of SP7 represents a third genetic cause of JPD

A Genome-Wide Association Study of Psoriasis and Psoriatic Arthritis Identifies New Disease Loci

A genome-wide association study was performed to identify genetic factors involved in susceptibility to psoriasis (PS) and psoriatic arthritis (PSA), inflammatory diseases of the skin and joints in humans. 223 PS cases (including 91 with PSA) were genotyped with 311,398 single nucleotide polymorphisms (SNPs), and results were compared with those from 519 Northern European controls. Replications were performed with an independent cohort of 577 PS cases and 737 controls from the U.S., and 576 PSA patients and 480 controls from the U.K.. Strongest associations were with the class I region of the major histocompatibility complex (MHC). The most highly associated SNP was rs10484554, which lies 34.7 kb upstream from HLA-C (P = 7.8×10−11, GWA scan; P = 1.8×10−30, replication; P = 1.8×10−39, combined; U.K. PSA: P = 6.9×10−11). However, rs2395029 encoding the G2V polymorphism within the class I gene HCP5 (combined P = 2.13×10−26 in U.S. cases) yielded the highest ORs with both PS and PSA (4.1 and 3.2 respectively). This variant is associated with low viral set point following HIV infection and its effect is independent of rs10484554. We replicated the previously reported association with interleukin 23 receptor and interleukin 12B (IL12B) polymorphisms in PS and PSA cohorts (IL23R: rs11209026, U.S. PS, P = 1.4×10−4; U.K. PSA: P = 8.0×10−4; IL12B:rs6887695, U.S. PS, P = 5×10−5 and U.K. PSA, P = 1.3×10−3) and detected an independent association in the IL23R region with a SNP 4 kb upstream from IL12RB2 (P = 0.001). Novel associations replicated in the U.S. PS cohort included the region harboring lipoma HMGIC fusion partner (LHFP) and conserved oligomeric golgi complex component 6 (COG6) genes on chromosome 13q13 (combined P = 2×10−6 for rs7993214; OR = 0.71), the late cornified envelope gene cluster (LCE) from the Epidermal Differentiation Complex (PSORS4) (combined P = 6.2×10−5 for rs6701216; OR 1.45) and a region of LD at 15q21 (combined P = 2.9×10−5 for rs3803369; OR = 1.43). This region is of interest because it harbors ubiquitin-specific protease-8 whose processed pseudogene lies upstream from HLA-C. This region of 15q21 also harbors the gene for SPPL2A (signal peptide peptidase like 2a) which activates tumor necrosis factor alpha by cleavage, triggering the expression of IL12 in human dendritic cells. We also identified a novel PSA (and potentially PS) locus on chromosome 4q27. This region harbors the interleukin 2 (IL2) and interleukin 21 (IL21) genes and was recently shown to be associated with four autoimmune diseases (Celiac disease, Type 1 diabetes, Grave's disease and Rheumatoid Arthritis)

Ecological Impact Prediction of Groundwater Change in Phreatic Aquifer under Multi-Mining Conditions

In aeolian sandy grass shoal catchment areas that rely heavily on groundwater, mining-induced geological deformation and aquifer drainage are likely to cause irreversible damage to natural groundwater systems and affect the original circulation of groundwater, thus threatening the ecological environment. This study aimed to predict the impact of groundwater level decline on vegetation growth in the Hailiutu River Basin (HRB), which is a coal-field area. Based on remote-sensing data, the land use/cover change was interpreted and analyzed, and the central areas of greensward land in the basin were determined. Subsequently, the correlation between groundwater depth and grassland distribution was analyzed. Then, the groundwater system under natural conditions was modeled using MODFLOW, and the groundwater flow field in 2029 was predicted by loading the generalized treatment of coal mine drainage water to the model. The change in groundwater depth caused by coal mining and its influence on the grassland were obtained. The results show that coal mining will decrease the groundwater depth, which would induce degradation risks in 4 of the original 34 aggregation centers of greensward land that originally depended on groundwater for growth in HRB because they exceeded the groundwater threshold. The prediction results show that the maximum settlement of groundwater level can reach 5 m in the northern (Yinpanhao), 6 m in the eastern (Dahaize), and 10 m in the southern (Balasu) region of HRB. Attention should be paid to vegetation degradation in areas where groundwater depth exceeds the minimum threshold for plant growth

Efficient and inexpensive MPCVD method to synthesize Co3O4/MoS2 heterogeneous composite materials with high stability for supercapacitors

Large-sized metal oxide particles have the potential to constitute cheap, high-performance, and high-stability supercapacitor electrode materials. Herein, the marketable large-sized Co3O4 particles (~6 [my]m) as the starting raw material, inexpensive Co3O4/MoS2 core-shell heterogeneous composites have been one-step fabricated via an improvised MPCVD system modified by a domestic microwave oven. After that, the surface morphology, composition structure, and valence state of elements were analyzed to the confirmed successful synthesis of MoS2 on the surface of Co3O4. Besides, the performance was tested by cyclic voltammetry and galvanostatic charge-discharge method. The results show that the synergistic effect of Co3O4 core and MoS2 shell can effectively improve the material's electrochemical performance. The specific capacitance of Co3O4/MoS2 composite can reach 337 F g-1 with a current density of 0.5 A g-1, which is six times more than the raw Co3O4 powder. Furthermore, it could maintain 93.6% of the initial specific capacitance after 2000 charges and discharges. Finally, the mechanism of material performance improvement is proposed